Skip to main content
Journal of Bacteriology logoLink to Journal of Bacteriology
. 1995 Nov;177(21):6316–6318. doi: 10.1128/jb.177.21.6316-6318.1995

Extreme resistance to thermally induced DNA backbone breaks in the hyperthermophilic archaeon Pyrococcus furiosus.

M J Peak 1, F T Robb 1, J G Peak 1
PMCID: PMC177479  PMID: 7592404

Abstract

Pyrococcus furiosus is a hyperthermophilic archaeon that grows optimally at 100 degrees C. It is not conceivable that these organisms could survive with genomic DNA that was subject to thermal destruction, yet the mechanisms protecting the genomes of this and other hyperthermophiles against such destruction are obscure. We have determined the effect of elevated temperatures up to 110 degrees C on the molecular weight of DNA in intact P. furiosus cells, compared with the effect of elevated temperatures on DNA in the mesothermophilic bacterium Escherichia coli. At 100 degrees C, DNA in P. furiosus cells is about 20 times more resistant to thermal breakage than that in E. coli cells, and six times fewer breaks were found in P. furiosus DNA after exposure to 110 degrees C for 30 min than in E. coli DNA at 95 degrees C. Our hypothesis for this remarkable stability of DNA in a hyperthermophile is that this hyperthermophile possesses DNA-binding proteins that protect against hydrolytic damage, as well as other endogenous protective mechanisms and DNA repair enzyme systems.

Full Text

The Full Text of this article is available as a PDF (209.9 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Brown S. H., Kelly R. M. Cultivation Techniques for Hyperthermophilic Archaebacteria: Continuous Culture of Pyrococcus furiosus at Temperatures near 100 degrees C. Appl Environ Microbiol. 1989 Aug;55(8):2086–2088. doi: 10.1128/aem.55.8.2086-2088.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Lindahl T., Andersson A. Rate of chain breakage at apurinic sites in double-stranded deoxyribonucleic acid. Biochemistry. 1972 Sep 12;11(19):3618–3623. doi: 10.1021/bi00769a019. [DOI] [PubMed] [Google Scholar]
  3. Lindahl T. Instability and decay of the primary structure of DNA. Nature. 1993 Apr 22;362(6422):709–715. doi: 10.1038/362709a0. [DOI] [PubMed] [Google Scholar]
  4. Lindahl T., Karlström O. Heat-induced depyrimidination of deoxyribonucleic acid in neutral solution. Biochemistry. 1973 Dec 4;12(25):5151–5154. doi: 10.1021/bi00749a020. [DOI] [PubMed] [Google Scholar]
  5. Lindahl T., Nyberg B. Heat-induced deamination of cytosine residues in deoxyribonucleic acid. Biochemistry. 1974 Jul 30;13(16):3405–3410. doi: 10.1021/bi00713a035. [DOI] [PubMed] [Google Scholar]
  6. Lindahl T., Nyberg B. Rate of depurination of native deoxyribonucleic acid. Biochemistry. 1972 Sep 12;11(19):3610–3618. doi: 10.1021/bi00769a018. [DOI] [PubMed] [Google Scholar]
  7. Noll K. M. Chromosome map of the thermophilic archaebacterium Thermococcus celer. J Bacteriol. 1989 Dec;171(12):6720–6725. doi: 10.1128/jb.171.12.6720-6725.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Peak M. J., Peak J. G. Single-strand breaks induced in Bacillus subtilis DNA by ultraviolet light: action spectrum and properties. Photochem Photobiol. 1982 May;35(5):675–680. doi: 10.1111/j.1751-1097.1982.tb02628.x. [DOI] [PubMed] [Google Scholar]
  9. Quaite F. E., Sutherland J. C., Sutherland B. M. Isolation of high-molecular-weight plant DNA for DNA damage quantitation: relative effects of solar 297 nm UVB and 365 nm radiation. Plant Mol Biol. 1994 Feb;24(3):475–483. doi: 10.1007/BF00024115. [DOI] [PubMed] [Google Scholar]
  10. Reeve J. N. Molecular biology of methanogens. Annu Rev Microbiol. 1992;46:165–191. doi: 10.1146/annurev.mi.46.100192.001121. [DOI] [PubMed] [Google Scholar]
  11. Sandman K., Grayling R. A., Dobrinski B., Lurz R., Reeve J. N. Growth-phase-dependent synthesis of histones in the archaeon Methanothermus fervidus. Proc Natl Acad Sci U S A. 1994 Dec 20;91(26):12624–12628. doi: 10.1073/pnas.91.26.12624. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Tuveson R. W., Peak J. G., Peak M. J. Single-strand DNA breaks induced by 365 NM radiation in Escherichia coli strains differing in sensitivity to near and far UV. Photochem Photobiol. 1983 Jan;37(1):109–112. doi: 10.1111/j.1751-1097.1983.tb04442.x. [DOI] [PubMed] [Google Scholar]
  13. Zwickl P., Fabry S., Bogedain C., Haas A., Hensel R. Glyceraldehyde-3-phosphate dehydrogenase from the hyperthermophilic archaebacterium Pyrococcus woesei: characterization of the enzyme, cloning and sequencing of the gene, and expression in Escherichia coli. J Bacteriol. 1990 Aug;172(8):4329–4338. doi: 10.1128/jb.172.8.4329-4338.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Bacteriology are provided here courtesy of American Society for Microbiology (ASM)

RESOURCES